Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population

by Vithana, E.N., Nongpiur, M.E., Venkataraman, D., Chan, S.H., Mavinahalli, J., Aung, T.
Published 2016

Therapeutic targeting of nuclear receptor corepressor misfolding in acute promyelocytic leukemia cells with genistein

by Ng, A.P.P., Nin, D.S., Fong, J.H., Venkataraman, D., Khan, M., Chen, C.-S.
Published 2011

Molecular evolution and phylogeny of elapid snake venom three-finger toxins

by Fry, B.G., Wüster, W., Kini, R.M., Brusic, V., Khan, A., Venkataraman, D., Rooney, A.P.
Published 2014

Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophy

by Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Yong, V.H.K., Aung, T., Tan, D.T.H.
Published 2011

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy

by Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Poh, R., Beuerman, R.W., Aung, T., Tan, D.T.H.
Published 2011

Association of TCF4 gene polymorphisms with Fuchs' corneal dystrophy in the Chinese

by Thalamuthu, A., Khor, C.C., Venkataraman, D., Koh, L.W., Tan, D.T.H., Aung, T., Mehta, J.S., Vithana, E.N.
Published 2014

Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in singaporean subjects

by Aung, T., Lim, M.C.C., Yong, V.H.K., Venkataraman, D., Toh, J.-Y., Vithana, E.N., Chew, P.T.K.
Published 2011

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese

by Lee, K.Y.C., Aung, T., Ho, S.L., Pek, D.C.K., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Vithana, E.N.
Published 2011

Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes

by Aung, T., Lim, M.C.C., Wong, T.T.L., Yong, V.H.K., Venkataraman, D., Venkatraman, A., Vithana, E.N., Chew, P.T.K., Thalamuthu, A.
Published 2011

A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy

by Lakshminarayanan, R., Vithana, E.N., Chai, S.-M., Chaurasia, S.S., Saraswathi, P., Venkatraman, A., Rojare, C., Venkataraman, D., Tan, D., Aung, T., Beuerman, R.W., Mehta, J.S.
Published 2014

Toll-like receptor 3 polymorphism rs3775291 is not associated with choroidal neovascularization or polypoidal choroidal vasculopathy in Chinese subjects

by Sng, C.C.A., Cackett, P.D., Yeo, I.Y., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Koh, A.H., Tai, E.-S., Wong, T.Y., Aung, T., Vithana, E.N.
Published 2014

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

by Vithana, E.N., Tan, D.T.H., Venkataraman, D., Venkatraman, A., Aung, T., Morgan, P.E., Casey, J.R., Ramprasad, V., Nagasamy, S., Kumaramanickevel, G., Rajagopal, R., Yam, G.H.F., Law, R.W.K., Pang, C.P., Yong, V.H.K
Published 2011